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Bacteriophages for Treating Urinary Tract Infections in Patients Undergoing Transurethral Resection of the Prostate

B

Balgrist University Hospital

Status and phase

Completed
Phase 3
Phase 2

Conditions

Intravesical Bacteriophage Treatment for Urinary Tract Infections

Treatments

Drug: Antibiotics
Biological: PYO Phage
Other: Sterile bacteriology media

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Urinary tract infections are among the most prevalent microbial diseases and their financial burden on society is substantial. The use of bacteriophages against bacterial pathogens has gained over the last years a renewed interest, because of the continuing increase in antibiotic resistance worldwide. Thus, the aim of this study is to investigate the efficacy of intravesical bacteriophage treatment to normalize urine culture compared to intravesical placebo or standard antibiotic treatment in a randomized controlled trial following a pilot phase.

Enrollment

97 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with urinary tract infections who are scheduled for transurethral resection of the prostate with urine culture (taken by mid-stream urine; or from the existing transurethral or suprapubic catheter) ≥104 colony forming units /mL of predefined uropathogens, including Enterococcus spp., Escherichia coli, Proteus mirabilis, Pseudomonas aeruginosa, Staphylococcus spp., and Streptococcus spp. and lower urinary tract symptoms such as urgency, frequency, dysuria, increased number of incontinence episodes
  • Written informed consent.

Exclusion criteria

  • Fever >38°C
  • CRP >100mg/L
  • Acute prostatitis
  • Concomitant fungal urinary tract infection
  • Current antibiotic treatment or antibiotic treatment within the last 7 days (exceptions: subjects with an active catheter associated urinary tract infection who have received prior antibiotics may be enrolled provided a minimum of 48 hours has elapsed between the last dose of the prior antibiotic and the time of obtaining the baseline urine specimen. Subjects receiving current antibiotic prophylaxis for catheter associated urinary tract infection who present signs and symptoms consistent with an active new catheter associated infection may be enrolled provided all other eligibility criteria are met including obtaining a pre-treatment qualifying baseline urine culture)
  • Any rapidly progressing disease or immediately life-threatening illness including but not limited to: acute hepatic failure, respiratory failure, and septic shock
  • No informed consent

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

97 participants in 3 patient groups, including a placebo group

Anbiotica
Active Comparator group
Treatment:
Drug: Antibiotics
Bacteriophages
Active Comparator group
Treatment:
Biological: PYO Phage
Placebo
Placebo Comparator group
Treatment:
Other: Sterile bacteriology media

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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